Metabolomics analysis reveals elevation of 3-indoxyl sulfate in plasma and brain during chemically-induced acute kidney injury in mice: Investigation of nicotinic acid receptor agonists

Journal Article · Mon Aug 15 00:00:00 EDT 2011 · Toxicology and Applied Pharmacology

DOI:https://doi.org/10.1016/j.taap.2011.05.015· OSTI ID:21587820

Chowdhury, Swapan ^[1]; Wirth, Mark ^[2]; Milburn, Michael V; Alexander, Danny C ^[3]; Alton, Kevin B ^[2]

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1. Drug Metabolism and Pharmacokinetics, Merck Research Laboratories, P.O. Box 2000, 126 E. Lincoln Avenue, Rahway, NJ 07065 (United States)
2. Drug Metabolism and Pharmacokinetics, Merck Research Laboratories, 2015 Galloping Hill Road, Kenilworth, NJ 07033 (United States)
3. Metabolon Inc., 800 Capitola Drive, Suite 1, Durham, NC, 27713 (United States)

An investigative renal toxicity study using metabolomics was conducted with a potent nicotinic acid receptor (NAR) agonist, SCH 900424. Liquid chromatography-mass spectrometry (LC-MS) and gas chromatography-mass spectrometry (GC-MS) techniques were used to identify small molecule biomarkers of acute kidney injury (AKI) that could aid in a better mechanistic understanding of SCH 900424-induced AKI in mice. The metabolomics study revealed 3-indoxyl sulfate (3IS) as a more sensitive marker of SCH 900424-induced renal toxicity than creatinine or urea. An LC-MS assay for quantitative determination of 3IS in mouse matrices was also developed. Following treatment with SCH 900424, 3IS levels were markedly increased in murine plasma and brain, thereby potentially contributing to renal- and central nervous system (CNS)-related rapid onset of toxicities. Furthermore, significant decrease in urinary excretion of 3IS in those animals due to compromised renal function may be associated with the elevation of 3IS in plasma and brain. These data suggest that 3IS has a potential to be a marker of renal and CNS toxicities during chemically-induced AKI in mice. In addition, based on the metabolomic analysis other statistically significant plasma markers including p-cresol-sulfate and tryptophan catabolites (kynurenate, kynurenine, 3-indole-lactate) might be of toxicological importance but have not been studied in detail. This comprehensive approach that includes untargeted metabolomic and targeted bioanalytical sample analyses could be used to investigate toxicity of other compounds that pose preclinical or clinical development challenges in a pharmaceutical discovery and development. - Research Highlights: > Nicotinic acid receptor agonist, SCH 900424, caused acute kidney injury in mice. > MS-based metabolomics was conducted to identify potential small molecule markers of renal toxicity. > 3-indoxyl-sulfate was found to be as a more sensitive marker of renal toxicity than creatinine or urea. > 3-IS levels were increased not only in murine plasma but also in the brain. > 3-IS potentially contributes to renal-and CNS-related rapid onset of toxicities.

• OSTI ID: 21587820
• Journal Information: Toxicology and Applied Pharmacology, Vol. 255, Issue 1; Other Information: DOI: 10.1016/j.taap.2011.05.015; PII: S0041-008X(11)00203-1; Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA); ISSN 0041-008X
• Country of Publication: United States
• Language: English

Related Subjects

60 APPLIED LIFE SCIENCES
ANIONS
BIOLOGICAL MARKERS
BLOOD
BRAIN
CREATININE
DRUGS
GAS CHROMATOGRAPHY
KIDNEYS
KYNURENINE
LIQUID COLUMN CHROMATOGRAPHY
MASS SPECTROSCOPY
MICE
NICOTINIC ACID
PLASMA
RATS
RECEPTORS
SULFATES
TOXICITY
TRYPTOPHAN
UREA
AMIDES
AMINO ACIDS
ANIMALS
AROMATICS
AZAARENES
AZINES
AZOLES
BIOLOGICAL MATERIALS
BODY
BODY FLUIDS
CARBONIC ACID DERIVATIVES
CARBOXYLIC ACIDS
CENTRAL NERVOUS SYSTEM
CHARGED PARTICLES
CHROMATOGRAPHY
HETEROCYCLIC ACIDS
HETEROCYCLIC COMPOUNDS
IMIDAZOLES
IMINES
INDOLES
IONS
KETO ACIDS
MAMMALS
MATERIALS
MEMBRANE PROTEINS
MONOCARBOXYLIC ACIDS
NERVOUS SYSTEM
ORGANIC ACIDS
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANS
OXYGEN COMPOUNDS
PROTEINS
PYRIDINES
PYRROLES
RODENTS
SEPARATION PROCESSES
SPECTROSCOPY
SULFUR COMPOUNDS
VERTEBRATES
VITAMIN B GROUP
VITAMINS